RE: Cohort 42 Feb 2025 08:41
It is sad that you think that those tricks would work. It really shows you understand very little about this space.
The major hurdle with the FDA is safety, with the FDA having higher tolerance when it comes to terminal diseases. With the phase 2 complete, that part is settled. They would go for a small biomarker equivalence followed by a randomised, if a serious contender decides to go ahead, they would have it marketed in 3 years.
Scancell trying to revive a dead patent without demonstrating clear superiority of iscib1+ vs scib1 in the same patient population isn't going to fool anyone that matters. Just you lot :)